Baylor Institute for Immunology Research, Baylor Research Institute, Dallas, TX 75204; and.
Immunobiology and Transplant Research, Houston Methodist Hospital and Houston Methodist Research Institute, Houston, TX 77030.
J Immunol. 2014 Aug 1;193(3):1364-72. doi: 10.4049/jimmunol.1303322. Epub 2014 Jul 2.
Many members of the DEXD/H box helicase family play important roles in the innate immune system against viral infection. Therefore, we isolated dsRNA complex in myeloid dendritic cells. We found that DHx15, a DEXDc helicase family member, is one of the components of this complex. Knockdown of DHX15 expression by short hairpin RNA efficiently reduced the ability of myeloid dendritic cells to produce IFN-β, IL-6, and TNF-α in response to dsRNA and RNA virus. DHX15 specifically bound polyinosine-polycytidylic acid via its helicase C-terminal domain. DHX15 interacted with MAVS and formed a complex following stimulation with polyinosine-polycytidylic acid. The N-terminal domain containing a DEXDc motif in DHX15 bound the C terminus of MAVS. DHX15 is required to activate IRF3 phosphorylation as well as NF-κB and MAPK signaling during RNA virus infection. We, therefore, identified DHX15 as a new RNA virus sensor mediated by MAVS to activate the immune responses to RNA.
DEXD/H 盒解旋酶家族的许多成员在抗病毒感染的先天免疫系统中发挥重要作用。因此,我们分离了髓样树突状细胞中的 dsRNA 复合物。我们发现,DEXDc 解旋酶家族成员 DHx15 是该复合物的成分之一。短发夹 RNA 敲低 DHX15 的表达可有效降低髓样树突状细胞产生 IFN-β、IL-6 和 TNF-α 的能力,以响应 dsRNA 和 RNA 病毒。DHX15 通过其解旋酶 C 端结构域特异性结合多聚肌苷酸-多聚胞苷酸。DHX15 与 MAVS 相互作用,并在多聚肌苷酸-多聚胞苷酸刺激后形成复合物。DHX15 中的 DEXDc 基序包含 N 端结构域,与 MAVS 的 C 端结合。DHX15 在 RNA 病毒感染过程中激活 IRF3 磷酸化以及 NF-κB 和 MAPK 信号通路是必需的。因此,我们将 DHX15 鉴定为一种新的 RNA 病毒传感器,该传感器通过 MAVS 介导激活对 RNA 的免疫反应。